A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617937



Internal ID21566242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65147241..65147241hg38UCSC Ensembl
chr3:65132916..65132916hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138811
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617937
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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